Lv11
45 积分 2021-10-11 加入
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBB
2小时前
求助中
Mutations in AMBRA1 aggravate β-thalassemia by impairing autophagy-mediated clearance of free α-globin
2小时前
已完结
Clinical outcomes of a genomic newborn screening study in Qingdao, China
2小时前
已完结
Targeted Disruption of the Mouse Mitoferrin (Slc25A37) Mitochondrial Solute Carrier Results in Defective Primitive and Definitive Erythropoiesis
1个月前
已关闭
Mitoferrin is essential for erythroid iron assimilation
1个月前
已完结
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBB
2个月前
已关闭
Clinical outcomes of a genomic newborn screening study in Qingdao, China
2个月前
已关闭
Genetics of age‐related hearing loss
4个月前
已完结
Urgent global opportunities to prevent birth defects
4个月前
已关闭
Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants
5个月前
已完结
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